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nsv6817892

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:117,687

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 631 SVs from 73 studies. See in: genome view    
    Submitted genomic2,591,694-2,709,380Question Mark
    Overlapping variant regions from other studies: 631 SVs from 73 studies. See in: genome view    
    Remapped(Score: Perfect):2,631,328-2,749,014Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6817892Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr72,591,6942,709,380
    nsv6817892RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr72,631,3282,749,014

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18542786deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18542786Submitted genomicNC_000007.14:g.259
    1694_2709380del
    GRCh38 (hg38)NC_000007.14Chr72,591,6942,709,380
    nssv18542786RemappedPerfectNC_000007.13:g.263
    1328_2749014del
    GRCh37.p13First PassNC_000007.13Chr72,631,3282,749,014

    No validation data were submitted for this variant

    No clinical assertion data were submitted for this variant

    Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

    Genotype Information

    Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
    nssv185427867e-062276044
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